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GNAS 基因不参与黑斑息肉病患者的胃肠道肿瘤形成。

GNAS is not involved in gastrointestinal tumour formation in Peutz-Jeghers syndrome.

机构信息

Department of Gastroenterology and Hepatology, Erasmus Medical University Centre, Room L-463, 's Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands.

出版信息

Fam Cancer. 2013 Sep;12(3):581-2. doi: 10.1007/s10689-013-9602-6.

Abstract

Peutz-Jeghers syndrome (PJS), caused by germ-line mutations in LKB1, is characterized by the development of hamartomatous polyps in the gastrointestinal (GI) tract. McCune Albright syndrome (MAS), caused by somatic activating mutations in GNAS, presents with cutaneous, skeletal, and endocrine manifestations. Recently, hamartomatous GI polyps with histological features similar to those in PJS were observed in MAS patients, suggesting a role for GNAS in the pathogenesis of PJS. This study reports the first somatic GNAS mutation analysis in GI tumours of PJS patients. No mutations were observed, suggesting that GNAS is not involved in the pathogenesis of GI tumours in PJS.

摘要

Peutz-Jeghers 综合征(PJS)由 LKB1 种系突变引起,其特征是胃肠道(GI)道出现错构瘤性息肉。McCune-Albright 综合征(MAS)由 GNAS 体激活突变引起,表现为皮肤、骨骼和内分泌表现。最近,在 MAS 患者中观察到具有与 PJS 相似组织学特征的错构瘤性 GI 息肉,提示 GNAS 在 PJS 的发病机制中起作用。本研究报告了首例 PJS 患者 GI 肿瘤的体细胞 GNAS 突变分析。未观察到突变,提示 GNAS 不参与 PJS 中 GI 肿瘤的发病机制。

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